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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4726 - 4750 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Drosophila melanogaster (fruit fly)
DOID:13223
  • uterine fibroid
  • Aliases:
    • Plexiform leiomyoma
    • UTERUS FIBROMA
    • leiomyoma of Corpus Uteri
    • uterine leiomyoma
Drosophila melanogaster (fruit fly)
DOID:0111547
  • retinal arterial tortuosity
  • Aliases:
    • RATOR
    • retinal arteriolar tortuosity
    • retinal hemorrhage with vascular tortuosity
    • tortuosity of retinal arteries
Drosophila melanogaster (fruit fly)
DOID:0110032
  • autosomal dominant Alport syndrome
Drosophila melanogaster (fruit fly)
DOID:0111740
  • X-linked deafness 6
  • Aliases:
    • DFNX6
Drosophila melanogaster (fruit fly)
DOID:10983
  • Alport syndrome
  • Aliases:
    • Hereditary Nephritis
Drosophila melanogaster (fruit fly)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Drosophila melanogaster (fruit fly)
DOID:0060263
  • porencephaly
Drosophila melanogaster (fruit fly)
DOID:0112314
  • brain small vessel disease 2
  • Aliases:
    • BSVD2
    • porencephaly 2
Mus musculus (house mouse)
DOID:10983
  • Alport syndrome
  • Aliases:
    • Hereditary Nephritis
Mus musculus (house mouse)
DOID:0110033
  • autosomal recessive Alport syndrome
Mus musculus (house mouse)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Mus musculus (house mouse)
DOID:0110032
  • autosomal dominant Alport syndrome
Mus musculus (house mouse)
DOID:14720
  • Ehlers-Danlos syndrome classic type 1
  • Aliases:
    • Ehlers-Danlos syndrome, type 1
    • type I Ehlers-Danlos syndrome
Mus musculus (house mouse)
DOID:0080726
  • Ehlers-Danlos syndrome classic type 2
Mus musculus (house mouse)
DOID:0050557
  • congenital muscular dystrophy
Mus musculus (house mouse)
DOID:0050558
  • Ullrich congenital muscular dystrophy
  • Aliases:
    • ULLRICH DISEASE
    • Ullrich scleroatonic muscular dystrophy
Mus musculus (house mouse)
DOID:2033
  • communication disorder
Mus musculus (house mouse)
DOID:0090050
  • dystonia 27
Mus musculus (house mouse)
DOID:0060642
  • recessive dystrophic epidermolysis bullosa
  • Aliases:
    • RDEB, Hallopeau-Siemens type
    • autosomal recessive dystrophic epidermolysis bullosa generalisata gravis
    • autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type
Mus musculus (house mouse)
DOID:4959
  • epidermolysis bullosa dystrophica
  • Aliases:
    • Dystrophic epidermolysis bullosa
Mus musculus (house mouse)
DOID:0080224
  • autosomal dominant dystrophic epidermolysis bullosa
Mus musculus (house mouse)
DOID:0111347
  • epidermolysis bullosa with congenital localized absence of skin and deformity of nails
  • Aliases:
    • EBD, Bart type
    • epidermolysis bullosa dystrophica, Bart type
Mus musculus (house mouse)
DOID:0080086
  • nonsyndromic congenital nail disorder 8
  • Aliases:
    • isolated toenail dystrophy
Mus musculus (house mouse)
DOID:0111345
  • transient bullous dermolysis of the newborn
  • Aliases:
    • DEB, bullous dermolysis of the newborn
    • DEB-BDN
Mus musculus (house mouse)
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024